CID 13987052

Details

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Internal ID 33d29b9b-a111-4308-b436-048400e768b7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids > Limonoids
IUPAC Name [(1R,2S,11R,12S,13R,16R,17R,19S)-17-acetyloxy-8-(furan-3-yl)-4,12-dihydroxy-1,9,11,16-tetramethyl-5,14-dioxapentacyclo[11.6.1.02,11.06,10.016,20]icos-9-en-19-yl] (E)-2-methylbut-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C33H44O9/c1-8-16(2)30(37)42-24-13-23(40-18(4)34)31(5)15-39-27-28(31)32(24,6)22-12-25(35)41-21-11-20(19-9-10-38-14-19)17(3)26(21)33(22,7)29(27)36/h8-10,14,20-25,27-29,35-36H,11-13,15H2,1-7H3/b16-8+/t20?,21?,22-,23+,24-,25?,27+,28?,29+,31+,32-,33+/m0/s1
InChI Key KQNNSYZQMSOOQH-NQUOODKUSA-N
Popularity 75 references in papers

Physical and Chemical Properties

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Molecular Formula C33H44O9
Molecular Weight 584.70 g/mol
Exact Mass 584.29853298 g/mol
Topological Polar Surface Area (TPSA) 125.00 Ų
XlogP 3.30
Atomic LogP (AlogP) 4.43
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 13987052

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9909 99.09%
Caco-2 - 0.7791 77.91%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7887 78.87%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7633 76.33%
OATP1B3 inhibitior + 0.9513 95.13%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9906 99.06%
P-glycoprotein inhibitior + 0.7735 77.35%
P-glycoprotein substrate + 0.6227 62.27%
CYP3A4 substrate + 0.7146 71.46%
CYP2C9 substrate - 0.7965 79.65%
CYP2D6 substrate - 0.8823 88.23%
CYP3A4 inhibition - 0.5415 54.15%
CYP2C9 inhibition - 0.7951 79.51%
CYP2C19 inhibition - 0.8712 87.12%
CYP2D6 inhibition - 0.9396 93.96%
CYP1A2 inhibition - 0.8291 82.91%
CYP2C8 inhibition + 0.7820 78.20%
CYP inhibitory promiscuity - 0.8185 81.85%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Danger 0.4898 48.98%
Eye corrosion - 0.9906 99.06%
Eye irritation - 0.9121 91.21%
Skin irritation - 0.5446 54.46%
Skin corrosion - 0.9421 94.21%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7189 71.89%
Micronuclear - 0.5400 54.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8730 87.30%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.5546 55.46%
Acute Oral Toxicity (c) I 0.7063 70.63%
Estrogen receptor binding + 0.8148 81.48%
Androgen receptor binding + 0.7049 70.49%
Thyroid receptor binding + 0.5402 54.02%
Glucocorticoid receptor binding + 0.7743 77.43%
Aromatase binding + 0.7186 71.86%
PPAR gamma + 0.7480 74.80%
Honey bee toxicity - 0.6125 61.25%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 1.0000 100.00%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.72% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.14% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.45% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.10% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.64% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 91.63% 90.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.60% 89.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 89.99% 81.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.21% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.32% 95.56%
CHEMBL2581 P07339 Cathepsin D 86.86% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.20% 94.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.26% 93.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.95% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.55% 97.14%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 83.34% 89.44%
CHEMBL3714130 P46095 G-protein coupled receptor 6 82.09% 97.36%
CHEMBL3401 O75469 Pregnane X receptor 81.60% 94.73%
CHEMBL340 P08684 Cytochrome P450 3A4 81.34% 91.19%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.23% 99.23%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Melia volkensii

Cross-Links

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PubChem 13987052
LOTUS LTS0271361
wikiData Q105144641